2 Graphical Abstract - Heterocyclic Letters

Transcription

ISSN: 2231 – 3087(print)
ISSN: 2230 – 9632 (Online)
Coden HLEEAI
Vol. 5: (1), 2015, 2-10
HL
http://heteroletters.org
Graphical Abstract
Heterocyclic Letters 5: iss.-1 (2015), 11-19
Synthesis of water soluble isoxazol-3-yl(isothiazol-3-yl) carboxamides and ureas containing amino acid residues – potential
anticancer agents
Vladimir I. Potkin,a* Alexey V. Kletskov,a Sergey K. Petkevich,a Svetlana G. Pashkevich,b Vladimir V. Kazbanov,b Andrew A.
Denisovb and Vladimir A. Kulchitskyb
a
Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, Surganova Str., 13, Minsk 220072, Belarus
Institute of Physiology, National Academy of Sciences of Belarus, Akademicheskaya Str., 28, Minsk, 220072, Belarus
E-mail: potkin@ifoch.bas-net.by
b
By reaction of accessible 5-(p-tolyl)isoxazole-, and 4,5-dichloroisothiazole-3-carbonyl azides with 4-aminobutanioc and 6-aminohexanoic
acids the corresponding substituted (1,2-azolyl)-3-carboxamides with amino acid residues were synthesized and transformed in water soluble
Na salt forms. For the synthesis of isothiazolyl(isoxazolyl)ureas with amino acid residues the 5-(p-tolyl)isoxazole-, 4,5-dichloroisothiazoleand 5-(benzylthio)-4-chloroisothiazole-3-carbonyl azides were converted into corresponding (1,2-azol-3-yl)carbamates by action of phenol
or 4-fluorophenol. Obtained carbamates were introduced in reaction with amino acids to form target substituted ureas, further transformed in
water soluble salt forms. Some of the synthesized derivatives possess antitumor activity.
Isolation and Characterization of Thiolutin from Streptomyces sp. Kib0393
Yingpan Song, Jie Zhang, Gang Chen*
College of Chemistry and Chemical Engineering, Xi’an Shiyou University, Xi’an, 710065, China
E-mail: gangchen@xsyu.edu.cn
O
HN
S
O
S
N
2
Heterocyclic Letters 5: iss.-1 (2015), 27- 36
Evaluation of highly active cytotoxic agents in the series of novel derivatives of N-hydroxy(and N-alkoxy)-ω
ω-(benzeneselanyl or 2benzoselenazolylsulfanyl)-alkaneamidines
Edgars Abele, Kira Rubina, Lena Golomba, Irina Shestakova, Elina Jaschenko, Veronika Bridane, Ramona Abele
Latvian Institute of Organic Synthesis, 21 Aizkraukles Street, Riga, LV-1006, Latvia
Synthesis
of
novel
derivatives
of
N-hydroxy
(and
N-alkoxy)-ω-(benzeneselanyl)alkaneamidines
and
2benzoselenazolylsulfanyl)alkaneamidines as potential cytotoxic agents was carried out in two or three steps. 6-(Benzoselenazol-2ylsulfanyl)-N-hydroxyhexanamidine exhibit high activity in vitro on monolayer tumor cell lines: MG-22A (mouse hepatoma) and HT-1080
(human fibrosarcoma).
Se
Ph
NH2
Ph
NH2
( )n
Se
N
O
NH2
PhSe
N
O
N
OMe
N
N
18-crown-6/ PhMe
/ K2CO3/ reflux
N
S
S
N
N
Me
N
N
S
Cl
N
Me
N
N
Ph
solid K2CO3/
18-crown-6 /
PhMe/ 25oC
NH2OH.HCl
Se ( )n CN
Ph
KOH/
EtOH
Br
Pd2(dba)3/
Xantphos/
Cs2CO3
DMF/ 130oC
Cl / Et3N
Cl
reflux
N O
Ph
Ph
N
Se
NH2
( )n
Se
NOH
O
N
S
Cl
( )n CN
Br
Ph SeH
MeI
I
N O
Se
HN
N
Cl
Br
N
SH
Se
( )n CN
N
S
solid K2CO3/
18-crown-6 /
PhMe/ 25oC
Se
( )n CN
NH2OH.HCl
N
KOH/
EtOH
Se
S
NH2
( )n
NOH
.
A green synthesis of thioxo pyrano[2, 3-d]pyrimidine using iron ore pellet as natural and reusable catalyst
Enayatollah Sheikhhosseini*, Malihe Faryabi
Department of Chemistry, Kerman Branch, Islamic Azad University, Kerman, Iran
*Corresponding author: sheikhhosseiny@gmail.com
Iron ore pellet is used as natural and reusable catalyst for a simple and efficient one-pot synthesis of thioxo pyrano[2,3-d]pyrimidine
derivatives via initial Knoevenagel, subsequent Micheal and final heterocyclization reactions of aryl aldehyde, malononitrile and
thiobarbituric acidin good to excellent yields.
O
S
O
Ar
CN
H
CN
HN
O
NH
O
Iron ore pellet
H2O
reflux
Ar
CN
HN
S
N
H
O
NH2
3
Retro synthesis and biological activity studies of thiazole-5-carboxylic acid amide derivatives
G. Naresh Kumara, S.Suneelab, K. Vasantha Kumar Pai*b
Department of Chemistry, Bharathiar University, Coimbatore-641046, India.
During the course of our investigation in the field of carboxylic acid antithrombotic agents, we have indentified and synthesized 2-[4'-(6,7dihydro-4H-thieno[3,2-c]pyridin-5-ylmethyl)-biphenyl-2-yl]-4-methyl-thiazole-5-carboxylic acid derivatives (9a-k), a carboxylic acid
derivatives with good in vivo activity. These findings prompted us to prepare new 2-[4'-(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-ylmethyl)biphenyl-2-yl]-4-methyl-thiazole-5-carboxylic acid derivatives (9a-k), in the hope of increasing activity and better understanding the
influence of ester and amides.
CN
Br
N
K2CO3
HN
S
CN
S
Methanol
MgCl2.6H2O
5
4
O
3
S
NaSH.H2O
O
ClO
NH2
N
Ethanol
O
S
N
N
S
S
O
6
vii7
OH
8
O
S
KOH
N
HN R
TEA O
N
SOCl2
HOBT
S
ACN
S
N
N
S
2
9a-k
A convenient synthesis of 3-(2-aryl amino)-ethylamino-2h-chromen-2-ones And their antimicrobial activities
Bethanamudi. Prasanna* and S. Kavitha
*Research center, Department of Chemistry, Chaitanya Degree & Post Graduate College (Autonomous), Kishanpura, Hanamkonda,
Warangal (TS)-506002.
E-Mail:prasschem@gmail.com.
A series of 3-(2-arylamino)ethylamino-2H-chromen-2-ones 5(a-f) have been synthesized from salyciladehyde and spectrally characterized.
In vitro antimicrobial activities of synthesized compounds were investigated against Grampositive S. Aureus bacteria, Gram-negative
E.Coli bacteria and fungi C. Albicans and A.Niger in comparison with standard drugs. Some of the tested compounds showed significant
antimicrobial activity.
R
OH
NH2
TEA
Methyl glycenate ester
1
4
NH
BrCH2CH2Br
O
O
H
3
O
amines
O
5(a-f)
O
NH
59
Synthesis, molecular docking and cytotoxic study of 7-methoxy-2-(3-methoxylphenyl)-1-benzofuran-5-carbaldehyde
7
carbaldehyde
Bapu R. Thorata, Ravindra Jagtapb, Vaishali B. Thoratc, Annasaheb Khemanard and Ramesh S. Yamgare
a. P. G. and Research centre, Ismail Yusuf Arts, Science and Commerce College, Jogeshwari (E), Mumbai 400060.
b. JJT University, Rajasthan.
c. IES, Junior College, Bandra (E), Mumbai.
d. Institute of Science, Fort, Mumbai
e. Patkar Varde College, Goregaon (W), Mumbai
benzofuran-5-carbaldehyde
carbaldehyde was synthesized by known literature method (Wittig reaction approach)
The 7-methoxy-2-(3-methoxylphenyl)-1-benzofuran
from vanillin. To deduce the anticancer and antibacterial activity of the 77-methoxy-2-(3-methoxylphenyl)-1-benzofuran
benzofuran-5-carbaldehyde, it is
docked with different
nt biomarkers of cancer cell and bacteria. Grid was generated for each oncoproteins by specifying the active site amino
acids. The binding model of best scoring analogue with each protein was assessed from their G-scores
G scores and disclosed by docking analysis
using
sing the XP visualizer tool. An analysis of the receptor-ligand
receptor
interaction studies revealed that 7-methoxy
methoxy-2-(3-methoxylphenyl)-1benzofuran-5-carbaldehyde
carbaldehyde is most active against 4FNY and 1VOM biomarkers and have the features to prove themselves as anticancer
anti
drugs. It shows strong cytotoxicity against human lung (A
(A-459) and breast (MCF-07) cell lines.
79
Antimicrobial evaluation of novel schiff’s bases
Purvesh J. Shah
Chemistry Department, K.K.Shah Jarodawala Maninagar Science College, Maninagar,
Ahmedabad, Gujarat (India).
*E-mail: purvesh23184@gmail.com
Schiff base is an important nitrogen containing compound. Many derivatives are prepared from its, which shows of various biologically as
well as pharmaceutical applications. Schiff bases are an important class, which constitute the building blocks of wide range of
pharmacologically active compounds. A series of novel schiff’s bases derivatives were synthesised and characterized by spectral studies in
present article. The novel synthesized compounds showed significant antimicrobial activity against various bacteria.
5
CsOH/γ-Al2O3 catalyzed mild and efficient method for the synthesis of novel multifunctionalized 4H-pyran derivatives via one-pot
three-component protocol.
MMV Ramana*, Rahul Betkar, Amey Nimkar, Prasanna Ranade, Balaji Mundhe
E mail: ramanammv@yahoo.com
The 4H- pyran derivatives were synthesized by a one-pot three-component reaction of an aromatic aldehyde, malononitrile, and ethyl
acetoacetate or isopropyl acetoacetate at room temperature in alcohol using recyclable CsOH/γ-Al2O3 as heterogeneous basic catalyst. The
characterization of CsOH/γ-Al2O3 catalyst was performed by using FT-IR, XRD, and TG-DTA techniques. The synthesized compounds
were characterized by UV, IR, NMR, and Elemental analysis.
Synthesis and antimicrobial evaluation of novel n-(4-(pyrrolidin-1-yl)benzylidene)-arylamine and diethyl ( arylamino)(4-(pyrrolidin1-yl)phenyl)methyl phosphonate
Sandeep D. Pardeshi, Jayant P. Sonar, S. A. Dokhe and Shivaji N. Thore*
Department of Chemistry, VinayakraoPatilMahavidyalaya, Vaijapur-423701
Email ID :snthore@rediffmail.com
In this work we have synthesis Schiff bases and α-amino phosphonates by conventional and non-conventional methods. The one pot
synthesis of α-amino phosphonates were also carried out by both the methods.
CHO
H2N
Ar
N
Ar
N
N
1
3a-3j
2
Tri ethyl Phosphite
Tri ethyl
Phosphite
H
N
Ar
N
O
O
P
O
4a-4j
6
Synthesis of N-Subtituted-2-Styrylquinazolin-4(3H)-ones under solvent free condition
Srinivasa Reddy1,2 Md. Rafeeq1, Ch. Venkata Ramana Reddy1 & P. K. Dubey1
1
Department of Chemistry, J N T University Hyderabad, College of Engineering, Hyderabad, 500 085. Telangana, India
Mahatma Gandhi Institute of Technology, Gandipet, Hyderabad-500075
E-mail: mohammadrafeeq8@gmail.com.
2
N-Subtituted-2-Styrylquinazolin-4(3H)-ones (5a-i) were synthesised from 2-methyl quinazolin-4(3H)-ones (2) with benzaldehydes followed
by alkylation with DMS, DES, PhCH2Cl (i.e. R= CH3, CH2CH3, CH2Ph), whole of the reactions are carried out in physical grinding under
solvent free conditions.
Synthesis and biological activity studies of quinoxaline derivatives
G. Naresh Kumara, S.Suneelab, K. Vasantha Kumar Pai*b
Department of Chemistry, Bharathiar University, Coimbatore-641046, India.
Various quinaoxalines were synthesized by the 1,2-diamines was the key intermediate for the synthesis of the new quinoxaline analogues, as
it was appropriately substituted with various amines using tetra hydro furan as base in dimethylsulfoxide afforded a series of novel
quinoxaline derivatives in good yields. The structures of all the newly synthesized molecules were assigned by spectral data. The
synthesized compounds were screened for their antibacterial activities strains using Cup–Plate method.
O
OH
H2N
IBX
80 0C, 45 min
THF , DMSO
H2N
i
N
N
ii
iiia-k
7
121
Synthesis of 3-(1-substituted-5-phenyl-4,5
4,5-dihydro-1H-pyrazol-3-yl)-4-substituted
substituted
insecticidal agents
benzo[4,5]imidazo[2,1-c][1,2,4]triazines
benzo[4,5]imidazo[2,1
as
Kanti Sharma* a, Lokesh Kumar Sharmaa and Renuka Jainb
a
Department of Chemistry, R.L. Saharia Govt. P.G. College, Kaladera, Jaipur
Jaipur-303 801, India
Department of Chemistry, University of Rajasthan, Jaipur-302
Jaipur
004, India
* E-mail: drkanti@gmail.com
b
An efficient, one pot, three component (1-(4
(4-substituted benzo[4,5]imidazo[2,1-c] [1,2,4] triazin-3-yl)
yl) ethanones 4, benzaldehyde and
hydrazino derivative), more sustainable and catalyst free reaction has been developed for the synthesis of 33-(1-substituted-5-phenyl-4,5dihydro-1H-pyrazol-3-yl)-4-substituted
substituted benzo[4,5]imidazo[2,1-c]
benzo[4,5]imidazo[2,1 [1,2,4]triazines 5-7 in glycerol.
8
Zinc acetate catalyzed an efficient synthesis of 2, 4, 5-triphenyl-1H-imidazole derivatives under solvent-free condition
V. P. Sondankar1*, N. R. Rathod1 and S. R. Bhusare2
1
Department of Chemistry, Phulsing Naik College, Pusad-445 216, MS, India
Department of Chemistry, Dnyanopasak College, Parbhani-431 401, MS, India
*Corresponding Author E-mail: vpsondankar@rediffmail.com
2
O
CHO
N
CH3COONH4
R
+
(CH3COO)2Zn
O R
1
N
H
2a-i
3a-i
Synthesis and characterization of some novel 4–[(substituted benzothiazol-2-yl) hydrazono]–3–methyl–5–(substituted
Phenyl imino)–4, 5–dihydroisoxazole
S. Sareen1, V. Khatri2, V. Sareen2
1
2
Vivekanand Institute of Technology (east), Department of Chemistry, Jaipur
Email : sareenparmod@yahoo.com
Department of Chemistry,University of Rajasthan, Jaipur
Synthesis of 2- [(4-fluorobenzothiazol-2-yl) hydrazono] butyric acid ethyl ester 3 from 2-Aminosubstituted benzothiazole and ethyl
acetoacetic ester in presence of HNO2 and ethanol has been described. 4-[(substituted benzothiazol-2-yl)-hydrazono]-3-methyl-4Hisoxazol-5-ones were prepared by the condensation of 2-[(substituted-benzothiazol-2-yl)-hydrazono]-3- oxobutyric acid ethyl ester in
ethanol with hydroxyl amine hydrochloride in the presence of sodium acetate.
N
NHN
R
CH3
S
N
O
O
N
NHN
R
CH3
S
N
N
O
R'
R= 4-Cl, 5-Cl, 4-F, 6-F
R'= 4-F, 2-F, 2-Cl, 2-CF3, 2,5-dichloro
5
9
Heterocyclic Letters 5: iss.-1 (2015), 143 -145
Palladium catalyzed selective monoarylation of 2-aminopyrimidines and 2-aminopyrazine with 1,2-dibromobenzene without
cyclization
Edgars Abele and Julija Visnevska
Latvian Institute of Organic Synthesis, 21 Aizkraukles Street, Riga, LV-1006, Latvia
A simple one-flask highly selective method for the Pd-catalyzed preparation of sterically hindered 2-(2-bromophenyl)pyrimidines.was
elaborated. 2-(2-Bromophenyl)pyrimidines were isolated in 22-64% yields. Similarly was prepared 2-(2-bromophenyl)aminopyrazine.
Scheme 1
N
R
N
1-3
N
R
X
N
N
H
Br
1a,b, 2a, 3a
N
NH2
4
R = H (1), R = Me (2), R = CF3 (3); X = CH (1a-c), X = N (1b)
10
N
Br , Pd(OAc)2 ,Cs2CO3 , PhMe
Xantphos, 110oC, 24h
N
X
Br
NH2
N
N
H
4a
Br

2 Graphical Abstract - Heterocyclic Letters

Transcription

Similar documents